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Prescription drugs recalled for contamination, potency or labelling.
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2,003 recalls · newest first
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
Sub-potent Drug
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
CGMP deviations
CGMP deviations
CGMP deviations
CGMP deviations
CGMP deviations
CGMP deviations
CGMP deviations
This product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect.
Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.
Subpotent drug: out of specification results
Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.
Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.
Failed Dissolution Specifications - did not meet the acceptance criteria for IVR Level 3 testing at 9 months 2-8¿C followed by 6 weeks at 25¿C
Presence of foreign substance.
Microbial Contamination of Non-Sterile Products: multiple Bacillus species organisms